Canonical Allele Identifier: CA511315953
Gene: GNAS HGNC NCBI
GNAS-AS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.57415714del (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.58840662del , CM000682.2:g.58840662del GRCh38
NC_000020.10:g.57415717del , CM000682.1:g.57415717del GRCh37
NC_000020.9:g.56849112del NCBI36
NG_016194.1:g.5923del
NG_021433.1:g.15245del
NG_016194.2:g.5923del

Transcript Alleles

HGVS Amino-acid Change
ENST00000419558.7:c.556del (GNAS) ENSP00000416234.2:p.Gln186ArgfsTer?
ENST00000453292.7:c.556del (GNAS) ENSP00000392000.2:p.Gln186ArgfsTer?
ENST00000419558.6:c.556del (GNAS) ENSP00000416234.2:p.Gln186ArgfsTer?
ENST00000453292.6:c.556del (GNAS) ENSP00000392000.2:p.Gln186ArgfsTer?
ENST00000657090.1:c.-39+722del (GNAS) ENSP00000499380.1:n.-39+722del
ENST00000667293.1:c.-27-188del (GNAS) ENSP00000499293.1:n.-27-188del
ENST00000313949.11:c.556del (GNAS) ENSP00000323571.7:p.Gln186ArgfsTer?
ENST00000371075.7:c.556del (GNAS) MANE Plus Clinical ENSP00000360115.3:p.Gln186ArgfsTer?
ENST00000371098.6:c.556del (GNAS) ENSP00000360139.2:p.Gln186ArgfsTer?
ENST00000419558.5:c.159del (GNAS)
ENST00000453292.5:c.319del (GNAS) ENSP00000392000.1:p.Gln107ArgfsTer?
NM_016592.2:c.556del (GNAS) NP_057676.1:p.Gln186ArgfsTer?
NM_016592.3:c.556del (GNAS) NP_057676.1:p.Gln186ArgfsTer?
NR_002785.2:n.819+1278del (GNAS-AS1)
XM_017027821.1:c.556del (GNAS) XP_016883310.1:p.Gln186ArgfsTer?
XM_017027822.1:c.556del (GNAS) XP_016883311.1:p.Gln186ArgfsTer?
XM_024451872.1:c.-182del (GNAS) XP_024307640.1:n.-182del
NM_016592.4:c.556del (GNAS) NP_057676.1:p.Gln186ArgfsTer?
NM_016592.5:c.556del (GNAS) MANE Plus Clinical NP_057676.1:p.Gln186ArgfsTer?